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+86-17702719238
sales@sun-shinechem.com
首页
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PI3K/Akt/mTOR
Epigenetics
Protein Tyrosine Kinase
Angiogenesis
Apoptosis
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Cytoskeletal Signaling
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Cas号索引 1
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Cas号索引 1
1402152-13-9 | Copanlisib HCl
(Catalog# : 18351)
Copanlisib也称为BAY 80 - 6946,是一个强有力的磷酸肌醇3-激酶(PI3K)抑制
19608-29-8 | CB-03-01
(Catalog# : 1712153)
CB-03-01, also known as cortexolone 17alpha-propionate, is a topical and peripherally
1797989-42-4 | CHIR99021 HCl
(Catalog# : 179825)
CHIR99021,又被称为 CT99021,是糖原合成酶激酶3β(GSK3β)抑制剂,
1005334-57-5 | CVT-10216
(Catalog# : 179818)
CVT-10216是强有力的和有选择性的,乙醛脱氢酶2(ALDH2)的可逆性抑
14513-15-6 | Cambinol
(Catalog# : 178313)
Cambinol是一种SIRT抑制剂。它能抑制促炎性细胞因子的表达,提高模
119671-47-5 | 2-吗啉-4-基-6-噻蒽-1-基吡喃-4-酮
(Catalog# : 1781504)
2-吗啉-4-基-6-噻蒽-1-基吡喃-4-酮;2-Chloro-6-morpholinopyran-4-one
1163719-56-9 | CCT196969
(Catalog# : 178913)
CCT196969,是一种pan-RAF / SFK抑制剂对治疗单纯的BRAF和NRAS突变型黑色
1846570-40-8 | CM-579
(Catalog# : 2017874)
CM-579是一种生物活性化学药品 。
1072946-52-1 | 5-氯-2-氰基苯硼酸
(Catalog# : 20178120)
5-氯-2-氰基苯硼酸
113359-04-9 | 头孢唑兰
(Catalog# : 17032402)
头孢唑兰(SCE 2787)是第四代头孢菌素。
122841-10-5 | 头孢噻利
(Catalog# : 17032401)
头孢噻利是一种广泛使用于β-内酰胺的抗生素。
1015474-32-4 | CC-122
(Catalog# : 17030313)
CC-122是一种具有潜在抗肿瘤活性的多向性通路调制器。
125314-13-8 | CP21R7
(Catalog# : 17022715)
CP21R7,也称CP21,是一个强有力的和选择性GSK-3β抑制剂。
1316215-12-9 | Citarinostat
(Catalog# : 17022701)
Citarinostat是一种HDAC6特异性抑制剂,HDAC6和HDAC3的IC50分别为4nM和76
147859-80-1 | CA-074 methyl ester (CA-074 Me)
(Catalog# : 17011104)
CA-074 Me是CA- 074的一种膜-渗透性衍生物,作为一种不可逆转的蛋白
1429639-50-8 | CZ415
(Catalog# : 17011101)
CZ415,是一种有效的ATP-竞争性mTOR抑制剂,拥有非常好的细胞渗透率
1628208-23-0 | CPI-455
(Catalog# : 17109005)
CPI-455是一种特殊的KDM5抑制剂,提高了H3K4三甲基化(H3K4me3)的全球水
199986-75-9 | CVT-313
(Catalog# : 16122923)
CVT-313 is a potent and selective inhibitor of CDK2 that prevents neointimal prolifer
1213669-91-0 | CTP354
(Catalog# : 16122922)
CTP354, also known as C-21191, a novel deuterated subtype-selective GABA(A) modulator
1198300-79-6 | Cerdulatinib (PRT062070)
(Catalog# : 16122917)
Cerdulatinib, also known as PRT2070 and PRT062070, is a n ovel, oral, dual spleen tyr
178946-89-9 | C-DIM12
(Catalog# : 16122915)
C-DIM12 is a novel synthetic activator of Nurr1. C-DIM12 induces dopaminergic gene ex
1813527-81-9 | CCG215022
(Catalog# : 16122914)
CCG215022 is a potent GRK2 and GRK5 inhibitor. CCG215022 exhibited nanomolar IC50 val
1439399-58-2 | CB-839
(Catalog# : 16122913)
CB-839 an is orally bioavailable inhibitor of glutaminase, with potential antineoplas
1477949-42-0 | CAY10683
(Catalog# : 16122912)
CAY10683, also known as Santacruzamate A, is a potent and selective histone deacetyla
1049741-55-0 | Cardiogenol C HCl
(Catalog# : 16122911)
Cardiogenol C is a diaminopyrimidine compound that induces the differentiation of MHC
193273-69-7 | Capromorelin tartrate
(Catalog# : 16122910)
Capromorelin, also known as CP-424,391, is a growth hormone secretagogue and ghrelin
1380087-89-7 | CPI-0610
(Catalog# : 16122738)
CPI-0610 is a potent and selective benzoisoxazoloazepine BET bromodomain inhibitor an
1884712-47-3 | CPI-637
(Catalog# : 16122737)
CPI-637 is a selective and cell-active benzodiazepinone CBP/EP300 bromodomain inhibit
1790895-25-8 | CeMMEC13
(Catalog# : 6111701)
CeMMEC13 is an isoquinolinone that selectively inhibits the second bromodomain of TAF
1429239-98-4 | CB1-IN-1
(Catalog# : 6111108)
CB1-IN-1 is a peripherally restricted CB1R antagonist, with Ki of 0.3 nM and 21 nM fo
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产品分类
信号通路
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
-- Protein Tyrosine Kinase
----
VEGFR
----
EGFR
----
PDGFR
----
IGF-1R
----
FLT3
----
FGFR
----
c-Kit
----
Src
----
ALK
----
Ephrin receptor
----
BTK
----
Trk receptor
----
c-Met/HGFR
----
Syk (Spleen tyrosine kinase)
----
TAM Receptor
----
ULK1
----
CSF-1R
----
TYK2
----
ROS Kinase
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Bcr-Abl
----
Src
----
ALK
----
Syk
----
FAK
----
BTK
----
HIF
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- Cytoskeletal Signaling
----
Akt
----
Bcr-Abl
----
PKC
----
FAK
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
-- TGF-beta/Smad
----
Bcr-Abl
----
PKC
----
ROCK
----
TGF-beta/Smad
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
-- Neuronal Signaling
----
COX
----
Histamine Receptor
----
Dopamine Receptor
----
Opioid Receptor
----
GABA Receptor
----
OX Receptor
----
Amyloid-β
----
5-HT Receptor
----
γ-secretase
----
Adrenergic Receptor
----
NMDA Receptor
----
GlyT1
----
Beta-secretase
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
-- GPCR & G Protein
----
Histamine Receptor
----
Dopamine Receptor
----
Opioid Receptor
----
Endothelin Receptor
----
SGLT
----
OX Receptor
----
CaSR
----
CXCR
----
Vasopressin Receptor
----
Glucagon Receptor
----
Prostaglandin Receptor
----
5-HT Receptor
----
Adrenergic Receptor
----
Cannabinoid Receptor
----
Sphingosine 1 Phosphate Receptor
----
PKA
----
Adenosine Receptor
----
GnRH
----
LPL Receptor
----
Sigma Receptor
----
Ras
----
mAChR
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
-- Metabolism
----
PPAR
----
P450
----
HSP
----
PDE
----
Factor Xa
----
Phospholipase
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
Parasite
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
NADPH-oxidase
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
-- Vitamin D Related
----
VD/VDR
-- Membrane Transporter/Ion Channel
----
BCRP
----
CFTR
----
EAAT2
----
GABA Receptor
----
HCN Channel
----
Monoamine Transporter
----
Na+/Ca2+ Exchanger
----
Na+/K+ ATPase
----
nAChR
----
Calcium Channel
----
Chloride Channel
----
CRAC Channel
----
GlyT1
----
iGluR
----
P2X Receptor
----
P-glycoprotein
----
Amino acid transporter
----
Monocarboxylate Transporter
----
Potassium Channel
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
-- PROTAC
----
Molecular Glues
抑制剂/受体激动剂
中间体
分子砌块
--
Aldehydes
--
Amines
--
Amino Acids
--
Anilines
--
Boronic Acids
--
Bromides
--
Carboxes
--
Catalysts
--
Chiral Compounds
--
Deuterated
--
Fluorides
--
Imidazoles
--
Indoles and Oxindoles
--
Iodos
--
Nitro Compounds
--
Oxazoles
--
Peg Linkers
--
Phenols
--
Piperidines
--
Pyridines
--
Pyrimidines
--
Quinolines
--
Sulfonamides
--
Thiazoles
--
Trifluoroborates
--
Other Azoles
--
Other Heterocycles
--
Other Building Blocks
--
On Sale
新产品
天然化合物
最新产品
2883540-92-7 | STX-478
(Catalog# : 20633)
STX-478 是第二代突变体选择性口服 PI3Ka 小分子变构抑制剂。
1421936-85-7 | Iclepertin (BI-425809)
(Catalog# : 24084)
Iclepertin(BI-425809)是一种口服的GlyT-1小分子抑制剂,用于治疗与
1990504-34-1 | Bomedemstat
(Catalog# : 24001)
Bomedemstat 是一种口服的、不可逆的赖氨酸特异性去甲基酶 1 (LSD1)
2892065-45-9 | PLX-4545
(Catalog# : 24111)
PLX-4545 是一种口服生物可利用的 IKZF2 分子胶降解剂,旨在破坏高
3034880-93-5 | VVD-130037 ( BAY-3605349 )
(Catalog# : 24110)
VVD-130037 (BAY-3605349) 是一种口服小分子 KEAP1 (INrf2) 激活剂。
681159-27-3 | CBR-5884
(Catalog# : 24109)
CBR 5884 是一种磷酸甘油酸脱氢酶 (PHGDH) 抑制剂,能够抑制过度表达
1998725-11-3 | JHU-083
(Catalog# : 24108)
JHU-083 选择性阻断大脑 CD11b+ 细胞中的谷氨酰胺酶活性,并防止慢
2251753-65-6 | LXH-3-71
(Catalog# : 24107)
LXH-3-71是一种新型“分子胶”,可诱导PHGDH和DDB1-CUL4泛素连接酶之
2259648-80-9 | CC-92480 ( Mezigdomide )
(Catalog# : 20510)
CC-92480 是一种有效的新型 CELMoD 化合物,旨在快速最大程度地降解
2394874-66-7 | Adrixetinib ( Q-702 )
(Catalog# : 20617)
Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag